The present invention comprises a sequence listing.

The present invention relates to recombinant host cells capable of producing various recombinant polypeptides, in particular enzymes, free from contaminating DNA, as well as methods of producing said polypeptides free from contaminating DNA.

Many Bacillus production strains are used for recombinant production of enzymes, and there are often regulatory restrictions concerning the presence of recombinant DNA in the final enzyme product.

A nuclease-encoding gene from Staphylococcus aureus was integrated into the genomes of several Poly(3-hydroxyalkanoates; PHA) producers and expressed, in order to express the nuclase and thereby reduce the otherwise high viscosity of cell-lysates due to the presence of chromosomal DNA. Staphylococcal nuclease was readily expressed in PHA-producing Pseudomonas strains and was directed to the periplasm, and occasionally to the culture medium, without affecting PHA production or strain stability [Zhuang et al. Reduction of Cell Lysate Viscosity during Processing of Poly(3-Hydroxyalkanoates) by Chromosomal Integration of the Staphylococcal Nuclease Gene in Pseudomonas putida. Appl Environ Microbiol. 1999 April; 65(4): 1524-1529].

The phosphate-starvation stimulon of Bacillus licheniformis has been analyzed at the transcriptional and translational level. It was shown that B. licheniformis has evolved its own strategies to cope with this nutrient limitation. By means of the secretome analysis a phytase was identified as the most abundant protein under phosphate-starvation conditions. Data of this study indicate that, unlike in B. subtilis, phosphate starvation in B. licheniformis does not induce the SigmaB-dependent general stress response (Hoi et al. The phosphate-starvation response of Bacillus licheniformis. 2006. Proteomics, Vol. 6 (12) pp. 3582-3601).

During phosphate starvation, Bacillus subtilis regulates genes in the PhoP regulon to reduce the cell's requirement for this essential substrate and to facilitate the recovery of inorganic phosphate from organic sources such as teichoic and nucleic acids. Among the proteins that are highly induced under these conditions is PstS, the phosphate-binding lipoprotein component of a high-affinity ABC-type phosphate transporter. PstS is encoded by the first gene in the pst operon, the other four members of which encode the integral membrane and cytoplasmic components of the transporter (Allenby et al. 2004. Post-transcriptional regulation of the Bacillus subtilis pst operon encoding a phosphate-specific ABC transporter. Microbiol 150 (Pt 8) pp. 2619-2628.

It is an object of the present invention to provide recombinant host cells capable of producing various products, in particular enzymes, free from DNA, as well as methods of producing various products free from DNA, and methods for constructing said recombinant host cells.

A recombinant Bacillus host cell was successfully engineered to express a recombinant nuclease (DNase) during fermentation, particularly towards the end of the fermentation.

We have cloned and expressed extracellular DNases from both Bacillus subtilis and Bacillus licheniformis that allow very efficient degradation of DNA. The gene nucB coding for this extracellular DNase (nuclease) from B. subtilis and B. licheniformis was cloned downstream of the pstS promoter. The pstS promoter is regulated by the level of phosphate in the medium during fermentation in a way where the promoter is activated by low levels of phosphate and blocked by high levels of phosphate.

Initially, flourescent protein GFP was used as a marker for expression from the pstS promoter, and it was shown that this particular promoter is very tightly controlled during fermentation. Since most Bacillus fermentations are entering a late phase where the level of phosphate is low, the expression of the nucB gene by the pstS promoter could be activated at the end of fermentation and express the nuclease when it is needed for cleaning the fermentation broth for excess DNA.

We show herein that an expression cassette consisting of the pstS promoter and nucB gene inserted into the chromosome of B. subtilis is regulated by the level of phosphate in shake flasks and 1 liter scale. In the presence of phosphate in the growth medium, the fermentation supernatant was not able to degrade added DNA. However, in a growth medium that was phosphate depleted by fermentation, a very efficient degradation of added DNA by the supernatant was observed, thus demonstrating the presence of nuclease in the supernatant. In this way we successfully separated the enzyme expression phase and the expression of the nuclease to avoid interference with enzyme productivity.

Accordingly, a first aspect of the invention relates to a cell producing at least one enzyme of interest and expressing one or more recombinant nuclease encoding gene(s) integrated into the genome of said cell, wherein the one or more recombinant nuclease encoding gene(s) is operably linked to a promoter foreign to the nucleotide sequence encoding the nuclease, thereby producing the nuclease(s) and the at least one enzyme of interest free from contaminating DNA.

In a second aspect, the invention relates to a method for producing an enzyme of interest free from contaminating DNA, said method comprising the steps of:

1. (a) cultivating a cell that produces at least one polypeptide of interest and expresses one or more recombinant nuclease encoding gene(s) integrated into the genome of said cell, wherein the one or more recombinant nuclease encoding gene(s) is operably linked to a promoter foreign to the nucleotide sequence encoding the nuclease, thereby producing the nuclease(s); and
2. (b) isolating the enzyme of interest.

• Fig. 1. A Northern blot showing expression of the pst-operon during a fermentation. The pst-operon in B. licheniformis consists of five genes (as in B. subtilis): pstS/C/A/BA/BB. The regulation seems to be the same as in B. subtilis, where the pst-operon is transcribed as a 4.4 kb primary transcript and is rapidly processed into smaller products, including a stable 0.9 kb pstS transcript.
• Fig. 2. Change in on-line emission spectra during 9 h of sampling in a fermentation, starting 4 hours before induction of phosphate starvation (for simplicity, one spectrum per hour is shown in this graph, but data was collected once every 10 minutes during the experiment). The peak at 460 to 480 nm is a reflection of the excitation light and the peak at 508 nm that increases with time is the GFP emission signal.
• Fig. 3. Data from samples taken out from a fermentation over a period of nine hours, showing on-line and off-line GFP determinations, growth of biomass, phosphate concentration, FACS analysis, alkaline phosphatase activity, and mRNA levels of the native pstS mRNA and the pstS-GFP fusion mRNA.
• Fig. 4. FACS analysis and microscopic examination of samples taken before and during induction of a phosphate starvation response showing that the whole population induce GFP expression (see fig. 2 for comparison to on-line and off-line GFP data). Column A) shows the FACS analysis; the Y-axes in the FACS graphs show the sideward scatter (reflection of excitation light measured at wavelength 488+/-10 nm), which is a measure of cell size (or of size of any particle present in the medium); the X-axes show the intensity of the fluorescence at 530+/-30 nm (FL1). The light source is a blue laser (wavelength 488 nm). Columns B and C) show microscopy pictures of the samples using a phase-contrast and a fluorescence microscope.
• Fig. 5. On-line measurement of GFP emission in fermentation BPN100 (values at 507-511 nm). Phosphate starvation starts at 31 h and the GFP signal increases (31-36 h) until about one hour after addition of phosphate. The added phosphate is probably consumed at about 42 h where the GFP signal again starts to increase.
• Fig. 6. On-line measurement of GFP emission in fermentations BPN101 and BPN102 (values at 507-511 nm). Phosphate starvation is detected after 10 hours in BPN101, while no induction is seen in the high phosphate fermentation until half of the fermentation broth is substituted with a medium lacking phosphate. This induces an increase in GFP emission, which is halted for three hours by addition of 0.5 g phosphate.
• Fig. 7. A xylose-induced integrative cloning vector expression system for Bacillus licheniformis denoted pAN238, the full DNA sequence of this plasmid is shown in SEQ ID NO: 1.
• Fig. 8. A cloning vector expression system denoted pAN167, the full DNA sequence of this plasmid is shown in SEQ ID NO: 6.
• Fig. 9. Shows the analysis of supernatants for Dnase, from different amylase-production strains comprising nucB: MOL2716, MOL2717, MOL2718; the fermentations are in TY-medium:
  • Lane 1: Marker DNA
  • Lane 2: Marker DNA + MOL2716 strain (+ phosphate)
  • Lane 3: Marker DNA + MOL2717 strain (+ phosphate)
  • Lane 4: Marker DNA + MOL2718 strain (+ phosphate)
  • Lane 5: Marker DNA + MOL2684 strain (+ phosphate)
  • Lane 6: Marker DNA + Sm-30 strain (+ phosphate)
  • Lane 7: Marker DNA + MOL2716 strain (- phosphate)
  • Lane 8: Marker DNA + MOL2717 strain (- phosphate)
  • Lane 9: Marker DNA + MOL2718 strain (- phosphate)
  • Lane 10: Marker DNA + MOL2684 strain (- phosphate)
  • Lane 11: Marker DNA + Sm-30 strain (- phosphate)
  • Lane 12: Marker DNA
• Fig. 10. Shows the analysis of supernatants for Dnase, from the amylase-production strain comprising nucB: MOL2717; the fermentations were in 1 liter scale, phosphate limited.
  • Lane 1: Marker DNA
  • Lane 2: Marker DNA + MOL2717 strain, 1 liter fermentation (- phosphate), 1. day
  • Lane 3: Marker DNA + MOL2717 strain, 1 liter fermentation (- phosphate), 2. day
  • Lane 4: Marker DNA + MOL2717 strain, 1 liter fermentation (- phosphate), 3. day
  • Lane 5: Marker DNA + MOL2717 strain, 1 liter fermentation (- phosphate), 4. day
  • Lane 6: Marker DNA + MOL2717 strain, 1 liter fermentation (- phosphate), 5. day
  • Lane 7: Marker DNA + MOL2717 strain, TY medium (- phosphate), overnight
  • Lane 8: Marker DNA + MOL2684 strain, TY medium (- phosphate), overnight
  • Lane 9: Marker DNA + Sm-30 strain, TY medium (- phosphate), overnight
  • Lane 10: Marker DNA + MOL2717 strain, PS1 medium, 7 days
  • Lane 11: Marker DNA + MOL2684 strain, PS1 medium, 7 days
  • Lane 12: Marker DNA + Sm-30 strain, PS1 medium, 7 days
  • Lane 13: Marker DNA

The first aspect of the invention relates to a cell producing at least one enzyme of interest and expressing one or more recombinant nuclease encoding gene(s) integrated into the genome of said cell, wherein the one or more recombinant nuclease encoding gene(s) is operably linked to a promoter foreign to the nucleotide sequence encoding the nuclease, thereby producing the nuclease(s).

Host cell: The term "host cell" or "cell", as used herein, includes any cell type which is susceptible to transformation, transfection, transduction, and the like with a nucleic acid construct comprising a polynucleotide of the present invention.

The present invention also relates to recombinant host cells, comprising a polynucleotide of the present invention, which are advantageously used in the recombinant production of the polypeptides. A vector comprising a polynucleotide of the present invention is introduced into a host cell so that the vector is maintained as a chromosomal integrant or as a self-replicating extra-chromosomal vector as described earlier. The term "host cell" encompasses any progeny of a parent cell that is not identical to the parent cell due to mutations that occur during replication. The choice of a host cell will to a large extent depend upon the gene encoding the polypeptide and its source.

The host cell is a Bacillus cell, e.g., Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus clausii, Bacillus coagulans, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus stearothermophilus, Bacillus subtilis, and Bacillus thuringiensis. In a preferred aspect, the bacterial host cell is a Bacillus lentus, Bacillus licheniformis, Bacillus stearothermophilus, or Bacillus subtilis cell. In another preferred aspect, the Bacillus cell is an alkalophilic Bacillus.

The introduction of a vector into a bacterial host cell may, for instance, be effected by protoplast transformation (see, e.g., Chang and Cohen, 1979, Molecular General Genetics 168: 111-115), using competent cells (see, e.g., Young and Spizizin, 1961, Journal of Bacteriology 81: 823-829, or Dubnau and Davidoff-Abelson, 1971, Journal of Molecular Biology 56: 209-221), electroporation (see, e.g., Shigekawa and Dower, 1988, Biotechniques 6: 742-751), or conjugation (see, e.g., Koehler and Thorne, 1987, Journal of Bacteriology 169: 5771-5278).

In a preferred embodiment of the invention, the cell is a Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus clausii, Bacillus coagulans, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus stearothermophilus, Bacillus subtilis, or Bacillus thuringiensis cell.

Isolated polypeptide: The term "isolated polypeptide" as used herein refers to a polypeptide which is at least 20% pure, preferably at least 40% pure, more preferably at least 60% pure, even more preferably at least 80% pure, most preferably at least 90% pure, and even most preferably at least 95% pure, as determined by SDS-PAGE.

Substantially pure polypeptide: The term "substantially pure polypeptide" denotes herein a polypeptide preparation which contains at most 10%, preferably at most 8%, more preferably at most 6%, more preferably at most 5%, more preferably at most 4%, at most 3%, even more preferably at most 2%, most preferably at most 1%, and even most preferably at most 0.5% by weight of other polypeptide material with which it is natively associated. It is, therefore, preferred that the substantially pure polypeptide is at least 92% pure, preferably at least 94% pure, more preferably at least 95% pure, more preferably at least 96% pure, more preferably at least 96% pure, more preferably at least 97% pure, more preferably at least 98% pure, even more preferably at least 99%, most preferably at least 99.5% pure, and even most preferably 100% pure by weight of the total polypeptide material present in the preparation.

The polypeptides of the present invention are preferably in a substantially pure form. In particular, it is preferred that the polypeptides are in "essentially pure form", i.e., that the polypeptide preparation is essentially free of other polypeptide material with which it is natively associated. This can be accomplished, for example, by preparing the polypeptide by means of well-known recombinant methods or by classical purification methods.

Herein, the term "substantially pure polypeptide" is synonymous with the terms "isolated polypeptide" and "polypeptide in isolated form."

In a preferred embodiment of the first and second aspects, the at least one polypeptide of interest comprises an enzyme, preferably the enzyme is a lyase, a ligase, a hydrolase, an oxidoreductase, a transferase, or an isomerase.

Allelic variant: The term "allelic variant" denotes herein any of two or more alternative forms of a gene occupying the same chromosomal locus. Allelic variation arises naturally through mutation, and may result in polymorphism within populations. Gene mutations can be silent (no change in the encoded polypeptide) or may encode polypeptides having altered amino acid sequences. An allelic variant of a polypeptide is a polypeptide encoded by an allelic variant of a gene.

Substantially pure polynucleotide: The term "substantially pure polynucleotide" as used herein refers to a polynucleotide preparation free of other extraneous or unwanted nucleotides and in a form suitable for use within genetically engineered protein production systems. Thus, a substantially pure polynucleotide contains at most 10%, preferably at most 8%, more preferably at most 6%, more preferably at most 5%, more preferably at most 4%, more preferably at most 3%, even more preferably at most 2%, most preferably at most 1%, and even most preferably at most 0.5% by weight of other polynucleotide material with which it is natively associated. A substantially pure polynucleotide may, however, include naturally occurring 5' and 3' untranslated regions, such as promoters and terminators. It is preferred that the substantially pure polynucleotide is at least 90% pure, preferably at least 92% pure, more preferably at least 94% pure, more preferably at least 95% pure, more preferably at least 96% pure, more preferably at least 97% pure, even more preferably at least 98% pure, most preferably at least 99%, and even most preferably at least 99.5% pure by weight. The polynucleotides of the present invention are preferably in a substantially pure form. In particular, it is preferred that the polynucleotides disclosed herein are in "essentially pure form", i.e., that the polynucleotide preparation is essentially free of other polynucleotide material with which it is natively associated. Herein, the term "substantially pure polynucleotide" is synonymous with the terms "isolated polynucleotide" and "polynucleotide in isolated form." The polynucleotides may be of genomic, cDNA, RNA, semisynthetic, synthetic origin, or any combinations thereof.

Nucleic acid construct: The term "nucleic acid construct" as used herein refers to a nucleic acid molecule, either single- or double-stranded, which is isolated from a naturally occurring gene or which is modified to contain segments of nucleic acids in a manner that would not otherwise exist in nature. The term nucleic acid construct is synonymous with the term "expression cassette" when the nucleic acid construct contains the control sequences required for expression of a coding sequence of the present invention.

Control sequence: The term "control sequences" is defined herein to include all components, which are necessary or advantageous for the expression of a polynucleotide encoding a polypeptide of the present invention. Each control sequence may be native or foreign to the nucleotide sequence encoding the polypeptide. Such control sequences include, but are not limited to, a leader, polyadenylation sequence, propeptide sequence, promoter, signal peptide sequence, and transcription terminator. At a minimum, the control sequences include a promoter, and transcriptional and translational stop signals. The control sequences may be provided with linkers for the purpose of introducing specific restriction sites facilitating ligation of the control sequences with the coding region of the nucleotide sequence encoding a polypeptide.

Operably linked: The term "operably linked" denotes herein a configuration in which a control sequence is placed at an appropriate position relative to the coding sequence of the polynucleotide sequence such that the control sequence directs the expression of the coding sequence of a polypeptide.

Coding sequence: When used herein the term "coding sequence" means a nucleotide sequence, which directly specifies the amino acid sequence of its protein product. The boundaries of the coding sequence are generally determined by an open reading frame, which usually begins with the ATG start codon or alternative start codons such as GTG and TTG. The coding sequence may a DNA, cDNA, or recombinant nucleotide sequence.

Expression: The term "expression" includes any step involved in the production of the polypeptide including, but not limited to, transcription, post-transcriptional modification, translation, post-translational modification, and secretion.

Expression vector: The term "expression vector" is defined herein as a linear or circular DNA molecule that comprises a polynucleotide encoding a polypeptide of the invention, and which is operably linked to additional nucleotides that provide for its expression.

A polypeptide of the present invention may be a bacterial polypeptide. For example, the polypeptide may be a gram positive bacterial polypeptide such as a Bacillus polypeptide, e.g., a Bacillus alkalophilus, Bacillus amyloliquefaciens, Bacillus brevis, Bacillus circulans, Bacillus coagulans, Bacillus lautus, Bacillus lentus, Bacillus licheniformis, Bacillus megaterium, Bacillus stearothermophilus, Bacillus subtilis, or Bacillus thuringiensis polypeptide; or a Streptomyces polypeptide, e.g., a Streptomyces lividans or Streptomyces murinus polypeptide; or a gram negative bacterial polypeptide, e.g., an E. coli or a Pseudomonas sp. polypeptide.

A polypeptide of the present invention may also be a fungal polypeptide, and more preferably a yeast polypeptide such as a Candida, Kluyveromyces, Pichia, Saccharomyces, Schizosaccharomyces, or Yarrowia polypeptide; or more preferably a filamentous fungal polypeptide such as an Acremonium, Aspergillus, Aureobasidium, Cryptococcus, Filobasidium, Fusarium, Humicola, Magnaporthe, Mucor, Myceliophthora, Neocallimastix, Neurospora, Paecilomyces, Penicillium, Piromyces, Schizophyllum, Talaromyces, Thermoascus, Thielavia, Tolypocladium, or Trichoderma polypeptide.

In another preferred aspect, the polypeptide is an Aspergillus aculeatus, Aspergillus awamori, Aspergillus fumigatus, Aspergillus foetidus, Aspergillus japonicus, Aspergillus nidulans, Aspergillus niger, Aspergillus oryzae, Fusarium bactridioides, Fusarium cerealis, Fusarium crookwellense, Fusarium culmorum, Fusarium graminearum, Fusarium graminum, Fusarium heterosporum, Fusarium negundi, Fusarium oxysporum, Fusarium reticulatum, Fusarium roseum, Fusarium sambucinum, Fusarium sarcochroum, Fusarium sporotrichioides, Fusarium sulphureum, Fusarium torulosum, Fusarium trichothecioides, Fusarium venenatum, Humicola insolens, Humicola lanuginosa, Mucor miehei, Myceliophthora thermophila, Neurospora crassa, Penicillium purpurogenum, Trichoderma harzianum, Trichoderma koningii, Trichoderma longibrachiatum, Trichoderma reesei, or Trichoderma viride polypeptide.

It will be understood that for the aforementioned species, the invention encompasses both the perfect and imperfect states, and other taxonomic equivalents, e.g., anamorphs, regardless of the species name by which they are known. Those skilled in the art will readily recognize the identity of appropriate equivalents.

Strains of these species are readily accessible to the public in a number of culture collections, such as the American Type Culture Collection (ATCC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), Centraalbureau Voor Schimmelcultures (CBS), and Agricultural Research Service Patent Culture Collection, Northern Regional Research Center (NRRL).

Furthermore, such polypeptides may be identified and obtained from other sources including microorganisms isolated from nature (e.g., soil, composts, water, etc.) using the above-mentioned probes. Techniques for isolating microorganisms from natural habitats are well known in the art. The polynucleotide may then be obtained by similarly screening a genomic or cDNA library of another microorganism. Once a polynucleotide sequence encoding a polypeptide has been detected with the probe(s), the polynucleotide can be isolated or cloned by utilizing techniques which are well known to those of ordinary skill in the art (see, e.g., Sambrook et al., 1989, supra).

Polypeptides of the present invention also include fused polypeptides or cleavable fusion polypeptides in which another polypeptide is fused at the N-terminus or the C-terminus of the polypeptide or fragment thereof. A fused polypeptide is produced by fusing a nucleotide sequence (or a portion thereof) encoding another polypeptide to a nucleotide sequence (or a portion thereof) of the present invention. Techniques for producing fusion polypeptides are known in the art, and include ligating the coding sequences encoding the polypeptides so that they are in frame and that expression of the fused polypeptide is under control of the same promoter(s) and terminator.

The techniques used to isolate or clone a polynucleotide encoding a polypeptide are known in the art and include isolation from genomic DNA, preparation from cDNA, or a combination thereof. The cloning of the polynucleotides of the present invention from such genomic DNA can be effected, e.g., by using the well known polymerase chain reaction (PCR) or antibody screening of expression libraries to detect cloned DNA fragments with shared structural features. See, e.g., Innis et al., 1990, PCR: A Guide to Methods and Application, Academic Press, New York. Other nucleic acid amplification procedures such as ligase chain reaction (LCR), ligated activated transcription (LAT) and nucleotide sequence-based amplification (NASBA) may be used.

Modification of a nucleotide sequence encoding a polypeptide of the present invention may be necessary for the synthesis of polypeptides substantially similar to the polypeptide. The term "substantially similar" to the polypeptide refers to non-naturally occurring forms of the polypeptide. These polypeptides may differ in some engineered way from the polypeptide isolated from its native source, e.g., artificial variants that differ in specific activity, thermostability, pH optimum, or the like. The variant sequence may be constructed on the basis of the nucleotide sequence presented as the polypeptide encoding region of SEQ ID NO: 1, e.g., a subsequence thereof, and/or by introduction of nucleotide substitutions which do not give rise to another amino acid sequence of the polypeptide encoded by the nucleotide sequence, but which correspond to the codon usage of the host organism intended for production of the enzyme, or by introduction of nucleotide substitutions which may give rise to a different amino acid sequence. For a general description of nucleotide substitution, see, e.g., Ford et al., 1991, Protein Expression and Purification 2: 95-107.

It will be apparent to those skilled in the art that such substitutions can be made outside the regions critical to the function of the molecule and still result in an active polypeptide. Amino acid residues essential to the activity of the polypeptide encoded by an isolated polynucleotide of the invention, and therefore preferably not subject to substitution, may be identified according to procedures known in the art, such as site-directed mutagenesis or alanine-scanning mutagenesis (see, e.g., Cunningham and Wells, 1989, Science 244: 1081-1085). In the latter technique, mutations are introduced at every positively charged residue in the molecule, and the resultant mutant molecules are tested for activity to identify amino acid residues that are critical to the activity of the molecule. Sites of substrate-enzyme interaction can also be determined by analysis of the three-dimensional structure as determined by such techniques as nuclear magnetic resonance analysis, crystallography or photoaffinity labelling (see, e.g., de Vos et al., 1992, Science 255: 306-312; Smith et al., 1992, Journal of Molecular Biology 224: 899-904; Wlodaver et al., 1992, FEBS Letters 309: 59-64).

The present invention also relates to nucleic acid constructs comprising an isolated polynucleotide of the present invention operably linked to one or more control sequences which direct the expression of the coding sequence in a suitable host cell under conditions compatible with the control sequences.

An isolated polynucleotide encoding a polypeptide of the present invention may be manipulated in a variety of ways to provide for expression of the polypeptide. Manipulation of the polynucleotide's sequence prior to its insertion into a vector may be desirable or necessary depending on the expression vector. The techniques for modifying polynucleotide sequences utilizing recombinant DNA methods are well known in the art.

The control sequence may be an appropriate promoter sequence, a nucleotide sequence which is recognized by a host cell for expression of a polynucleotide encoding a polypeptide of the present invention. The promoter sequence contains transcriptional control sequences which mediate the expression of the polypeptide. The promoter may be any nucleotide sequence which shows transcriptional activity in the host cell of choice including mutant, truncated, and hybrid promoters, and may be obtained from genes encoding extracellular or intracellular polypeptides either homologous or heterologous to the host cell.

Examples of suitable promoters for directing the transcription of the nucleic acid constructs of the present invention, especially in a bacterial host cell, are the promoters obtained from the E. coli lac operon, Streptomyces coelicolor agarase gene (dagA), Bacillus subtilis levansucrase gene (sacB), Bacillus licheniformis alpha-amylase gene (amyL), Bacillus stearothermophilus maltogenic amylase gene (amyM), Bacillus amyloliquefaciens alpha-amylase gene (amyQ), Bacillus licheniformis penicillinase gene (penP), Bacillus subtilis xylA and xylB genes, and prokaryotic beta-lactamase gene (Villa-Kamaroff et al., 1978, Proceedings of the National Academy of Sciences USA 75: 3727-3731), as well as the tac promoter (DeBoer et al., 1983, Proceedings of the National Academy of Sciences USA 80: 21-25). Further promoters are described in "Useful proteins from recombinant bacteria" in Scientific American, 1980, 242: 74-94; and in Sambrook et al., 1989, supra.

The control sequence may also be a suitable transcription terminator sequence, a sequence recognized by a host cell to terminate transcription. The terminator sequence is operably linked to the 3' terminus of the nucleotide sequence encoding the polypeptide. Any terminator which is functional in the host cell of choice may be used in the present invention.

The control sequence may also be a suitable leader sequence, a nontranslated region of an mRNA which is important for translation by the host cell. The leader sequence is operably linked to the 5' terminus of the nucleotide sequence encoding the polypeptide. Any leader sequence that is functional in the host cell of choice may be used in the present invention.

The control sequence may also be a polyadenylation sequence, a sequence operably linked to the 3' terminus of the nucleotide sequence and which, when transcribed, is recognized by the host cell as a signal to add polyadenosine residues to transcribed mRNA. Any polyadenylation sequence which is functional in the host cell of choice may be used in the present invention.

The control sequence may also be a signal peptide coding region that codes for an amino acid sequence linked to the amino terminus of a polypeptide and directs the encoded polypeptide into the cell's secretory pathway. The 5' end of the coding sequence of the nucleotide sequence may inherently contain a signal peptide coding region naturally linked in translation reading frame with the segment of the coding region which encodes the secreted polypeptide. Alternatively, the 5' end of the coding sequence may contain a signal peptide coding region which is foreign to the coding sequence. The foreign signal peptide coding region may be required where the coding sequence does not naturally contain a signal peptide coding region. Alternatively, the foreign signal peptide coding region may simply replace the natural signal peptide coding region in order to enhance secretion of the polypeptide. However, any signal peptide coding region which directs the expressed polypeptide into the secretory pathway of a host cell of choice may be used in the present invention.

Effective signal peptide coding regions for bacterial host cells are the signal peptide coding regions obtained from the genes for Bacillus NCIB 11837 maltogenic amylase, Bacillus stearothermophilus alpha-amylase, Bacillus licheniformis subtilisin, Bacillus licheniformis beta-lactamase, Bacillus stearothermophilus neutral proteases (nprT, nprS, nprM), and Bacillus subtilis prsA. Further signal peptides are described by Simonen and Palva, 1993, Microbiological Reviews 57: 109-137.

The control sequence may also be a propeptide coding region that codes for an amino acid sequence positioned at the amino terminus of a polypeptide. The resultant polypeptide is known as a proenzyme or propolypeptide (or a zymogen in some cases). A propolypeptide is generally inactive and can be converted to a mature active polypeptide by catalytic or autocatalytic cleavage of the propeptide from the propolypeptide. The propeptide coding region may be obtained from the genes for Bacillus subtilis alkaline protease (aprE), Bacillus subtilis neutral protease (nprT), Saccharomyces cerevisiae alpha-factor, Rhizomucor miehei aspartic proteinase, and Myceliophthora thermophila laccase (WO 95/33836).

Where both signal peptide and propeptide regions are present at the amino terminus of a polypeptide, the propeptide region is positioned next to the amino terminus of a polypeptide and the signal peptide region is positioned next to the amino terminus of the propeptide region.

It may also be desirable to add regulatory sequences which allow the regulation of the expression of the polypeptide relative to the growth of the host cell. Examples of regulatory systems are those which cause the expression of the gene to be turned on or off in response to a chemical or physical stimulus, including the presence of a regulatory compound. Regulatory systems in prokaryotic systems include the lac, tac, and trp operator systems. Other examples of regulatory sequences are those which allow for gene amplification. In these cases, the nucleotide sequence encoding the polypeptide would be operably linked with the regulatory sequence.

The present invention also relates to recombinant expression vectors comprising a polynucleotide of the present invention, a promoter, and transcriptional and translational stop signals. The various nucleic acids and control sequences described above may be joined together to produce a recombinant expression vector which may include one or more convenient restriction sites to allow for insertion or substitution of the nucleotide sequence encoding the polypeptide at such sites. Alternatively, a nucleotide sequence of the present invention may be expressed by inserting the nucleotide sequence or a nucleic acid construct comprising the sequence into an appropriate vector for expression. In creating the expression vector, the coding sequence is located in the vector so that the coding sequence is operably linked with the appropriate control sequences for expression.

The recombinant expression vector may be any vector (e.g., a plasmid or virus) which can be conveniently subjected to recombinant DNA procedures and can bring about expression of the nucleotide sequence. The choice of the vector will typically depend on the compatibility of the vector with the host cell into which the vector is to be introduced. The vectors may be linear or closed circular plasmids.

The vector may be an autonomously replicating vector, i.e., a vector which exists as an extrachromosomal entity, the replication of which is independent of chromosomal replication, e.g., a plasmid, an extrachromosomal element, a minichromosome, or an artificial chromosome. The vector may contain any means for assuring self-replication. Alternatively, the vector may be one which, when introduced into the host cell, is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. Furthermore, a single vector or plasmid or two or more vectors or plasmids which together contain the total DNA to be introduced into the genome of the host cell, or a transposon may be used.

The vectors of the present invention preferably contain one or more selectable markers which permit easy selection of transformed cells. A selectable marker is a gene the product of which provides for biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs, and the like.

A conditionally essential gene may function as a non-antibiotic selectable marker. Non-limiting examples of bacterial conditionally essential non-antibiotic selectable markers are the dal genes from Bacillus subtilis, Bacillus licheniformis, or other Bacilli, that are only essential when the bacterium is cultivated in the absence of D-alanine. Also the genes encoding enzymes involved in the turnover of UDP-galactose can function as conditionally essential markers in a cell when the cell is grown in the presence of galactose or grown in a medium which gives rise to the presence of galactose. Non-limiting examples of such genes are those from B. subtilis or B. licheniformis encoding UTP-dependent phosphorylase (EC 2.7.7.10), UDP-glucose-dependent uridylyltransferase (EC 2.7.7.12), or UDP-galactose epimerase (EC 5.1.3.2). Also a xylose isomerase gene such as xylA, of Bacilli can be used as selectable markers in cells grown in minimal medium with xylose as sole carbon source. The genes necessary for utilizing gluconate, gntK, and gntP can also be used as selectable markers in cells grown in minimal medium with gluconate as sole carbon source. Other examples of conditionally essential genes are known in the art. Antibiotic selectable markers confer antibiotic resistance to such antibiotics as ampicillin, kanamycin, chloramphenicol, erythromycin, tetracycline, neomycin, hygromycin or methotrexate.

The vectors of the present invention preferably contain an element(s) that permits integration of the vector into the host cell's genome or autonomous replication of the vector in the cell independent of the genome.

For integration into the host cell genome, the vector may rely on the polynucleotide's sequence encoding the polypeptide or any other element of the vector for integration into the genome by homologous or nonhomologous recombination. Alternatively, the vector may contain additional nucleotide sequences for directing integration by homologous recombination into the genome of the host cell at a precise location(s) in the chromosome(s). To increase the likelihood of integration at a precise location, the integrational elements should preferably contain a sufficient number of nucleic acids, such as 100 to 10,000 base pairs, preferably 400 to 10,000 base pairs, and most preferably 800 to 10,000 base pairs, which have a high degree of identity with the corresponding target sequence to enhance the probability of homologous recombination. The integrational elements may be any sequence that is homologous with the target sequence in the genome of the host cell. Furthermore, the integrational elements may be non-encoding or encoding nucleotide sequences. On the other hand, the vector may be integrated into the genome of the host cell by nonhomologous recombination.

For autonomous replication, the vector may further comprise an origin of replication enabling the vector to replicate autonomously in the host cell in question. The origin of replication may be any plasmid replicator mediating autonomous replication which functions in a cell. The term "origin of replication" or "plasmid replicator" is defined herein as a nucleotide sequence that enables a plasmid or vector to replicate in vivo.

Examples of bacterial origins of replication are the origins of replication of plasmids pBR322, pUC19, pACYC177, and pACYC184 permitting replication in E. coli, and pUB110, pE194, pTA1060, and pAMβ1 permitting replication in Bacillus.

More than one copy of a polynucleotide of the present invention may be inserted into the host cell to increase production of the gene product. An increase in the copy number of the polynucleotide can be obtained by integrating at least one additional copy of the sequence into the host cell genome or by including an amplifiable selectable marker gene with the polynucleotide where cells containing amplified copies of the selectable marker gene, and thereby additional copies of the polynucleotide, can be selected for by cultivating the cells in the presence of the appropriate selectable agent.

The procedures used to ligate the elements described above to construct the recombinant expression vectors of the present invention are well known to one skilled in the art (see, e.g., Sambrook et al., 1989, supra).

In a preferred embodiment of the invention, the one or more recombinant nuclease encoding gene(s) is integrated into the genome of said cell. This may be achieved as outlined herein or as disclosed in WO 2002/000907.

In another preferred embodiment of the invention the one or more recombinant nuclease encoding gene(s) is transcribed from a regulated promoter that is at least 10% upregulated, preferably at least 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100% or more upregulated, during the time of a standard fed-batch fermentation of said cell, even more preferably the promoter is upregulated in response to a substance-limitation in the growth medium, most preferably the promoter is upregulated in response to phosphate-limitation in the growth medium.

In a most preferred embodiment of the invention, the one or more recombinant nuclease encoding gene(s) is transcribed from the pstS promoter of B. licheniformis or B. subtilis.

In the production methods of the present invention, the cells are cultivated in a nutrient medium suitable for production of the polypeptide using methods well known in the art. For example, the cell may be cultivated by shake flask cultivation, and small-scale or large-scale fermentation (including continuous, batch, fed-batch, or solid state fermentations) in laboratory or industrial fermentors performed in a suitable medium and under conditions allowing the polypeptide to be expressed and/or isolated. The cultivation takes place in a suitable nutrient medium comprising carbon and nitrogen sources and inorganic salts, using procedures known in the art. Suitable media are available from commercial suppliers or may be prepared according to published compositions (e.g., in catalogues of the American Type Culture Collection). If the polypeptide is secreted into the nutrient medium, the polypeptide can be recovered directly from the medium. If the polypeptide is not secreted, it can be recovered from cell lysates.

The polypeptides may be detected using methods known in the art that are specific for the polypeptides. These detection methods may include use of specific antibodies, formation of an enzyme product, or disappearance of an enzyme substrate. For example, an enzyme assay may be used to determine the activity of the polypeptide as described herein.

The resulting polypeptide may be recovered using methods known in the art. For example, the polypeptide may be recovered from the nutrient medium by conventional procedures including, but not limited to, centrifugation, filtration, extraction, spray-drying, evaporation, or precipitation.

The polypeptides of the present invention may be purified by a variety of procedures known in the art including, but not limited to, chromatography (e.g., ion exchange, affinity, hydrophobic, chromatofocusing, and size exclusion), electrophoretic procedures (e.g., preparative isoelectric focusing), differential solubility (e.g., ammonium sulfate precipitation), SDS-PAGE, or extraction (see, e.g., Protein Purification, J.-C. Janson and Lars Ryden, editors, VCH Publishers, New York, 1989).

When following gene regulation in lab. scale fermentations using DNA microarrays, a number cellular responses are seen as a consequence of the changing fermentation medium.

Phosphate starvation in late stage fermentation samples was detected already in our first microarray experiments, using partial B. licheniformis microarray slides containing about 200 interesting genes. Cells are not "truly" limited for phosphate, since huge amounts of phosphate is normally incorporated into teichoic acids in the cell wall. When the cells sense a low concentration of phosphate in the medium, one of the responses is to substitute these teichoic acids with non-phosphate containing teichuronic acids and thereby liberate phosphate.

Making a biosensor for phosphate limitation could therefore be questioned, if only one biosensor was planned to be made. However, in combination with biosensors for different trace metals, the phosphate starvation biosensor is essential, as discussed above. A number of other facts also made the phosphate biosensor a very attractive choice to start with:

1. 1) the pst-operon (involved in high affinity uptake of phosphate) is very tightly regulated, i.e. the background level of transcription in cells that are not starved for phosphate is minimal and the transcription is very high when the cells are subjected to phosphate starvation (see fig. 1).
2. 2) Another gene that is induced during phosphate starvation is the phoD gene, which encodes an alkaline phosphatese/phosphodiesterase. The activity of this alkaline phosphatase is easy to measure (colorless paranitrophenol is hydrolyzed to free paranitrophenol, which is colored yellow) and thus gives a possibility to confirm results seen with the pstS-GFP fusion.
3. 3) Inorganic phosphate concentrations are easily determined with commercial kits or by HPCE. The reason for this is that phosphate is a major bioelement and phosphate starvation is induced already at about 0.5 g/L.

When the phosphate level is low the transcription of certain genes responds strongly. A set of such genes are found in the pst operon of Bacillus. In our experiment a gene encoding a variant of the green fluorescent protein, denoted BioST (variant: F64L, S65T), from the jellyfish Aequorea victoria, has been fused transcriptionally to the pst transcript [New Unstable Variants of Green Fluorescent Protein for studies of Transient gene expression in bacteria. App. Env. Mic. 1998 p2240-2246, incorporated herein by reference].

Constructs were made, wherein the bioST gene was inserted 1) immediately downstream of the pst promoter region and upstream of the pst operon "Ppst bioST", or 2) downstream of the last gene in the operon (pstBB) in the transcript "pstBB bioST'.

The Ppst bioST fusion was inserted into the chromosome of B. subtilis in the amyE locus (PP2203-1), and in B.licheniformis the fusion gene was inserted in the bglC gene (PP2244), using standard methods.

The pstBB bioST transcriptional fusion was inserted into the pst operon in the chromosome of another B.subtilis strain (PP2216-1), using standard methods.

The DNA sequences used in the pst constructs in B.subtilis was from the published B.subtilis 168 genome. The DNA sequences used in the pst constructs in B.licheniformis were isolated from a proprietary B.licheniformis Si3 strain.

The terminator behind bioST in both PP2203-1 and PP2244-1 is the aprH terminator from B.clausii. In the C-terminal insertion of bioST in PP2216-1 the terminator is the original terminator of the pst operon.

In the above strains the GFP accumulation may be a disadvantage to see what's going on in fermentation in the present moment - as the first step in that direction we made a BioST variant with an instability tag, the ssrA tag, which directs the cytoplasmatic peptides towards the clpX clpP degradation complex.

The ssrA tag from B.subtilis is known to be GKTNSFNQNVALLA. And the homologue from B.licheniformis Si3 is VKTHLNITGKSNQNLALAA.

A B.subtilis strain with the C-terminal B.subtilis ssrA tag on BioST was made. The GFP accumulation in B.subtilis PP2239-1 is much lower than the parallel PP2203-1 strain run under same conditions.

• PP2203-1: B.subtilis 168 aprE, nprE, amyE:(cat)Ppst bioST.
• PP2216-1: B.subtilis 168 aprE, nprE, pstBB' ::bioST.
• PP2244-1: B.licheniformis Si3 aprL,bglC::Ppst bioST.
• PP2239-1: B.subtilis 168 aprE, nprE, amyE:(cat)Ppst bioST_ssrA.

1. 1) A spectrometer, which detects all emission wavelengths between 329-1100 nm (AVANTES™ AVASPEC™-2048FT-SPU), coupled via an via an optic cable (AVANTES™ FC-UV600-2) to a collimating lens situated in a light protected box (see below). BioST emission maximum is at about 508 nm
2. 2) A light source, which gives a strong excitation light at about 470 nm and no light at all at wavelengths above 500 nm, since reflection of the excitation light into the spectrometer will disturb detection of the emission light of the GFP protein (BioST excitation maximum is at about 470 nm). We tested the AVANTES™ AVALIGHT™-LED-470 nm, with an optical bandpass filter (470+/-10 nm from KNIGHT OPTICAL™ (UK) Ltd), but found the light intensity too low. Instead we used a home-made light source, which consists of a 5 mm high brightness blue LED (2000 mcd, peak wavelength of 470 nm), combined with the abovementioned optical filter. The LED was placed in the light protected box, very close to the flow-through cuvette.
3. 3) A flow-through cuvette, through which fermentation broth is passed and then recirculated back to the tank. The circulation is driven by a peristaltic pump.
4. 4) A light-protected box (home-made), where the flow-through cuvette, the collimating lens, and the light source are mounted in angles that result in maximal detection of the emission signal.

To be able to use a biosensor for fermentation regulation, a number of important criteria have to be fulfilled:

1. 1) it must be possible to detect the signal of the cellular response to the starvation condition very soon after the cells first sense the starvation.
2. 2) the whole population should react in the same manner, so that regulation is not based on a reaction occurring in a sub-population of the cells.
3. 3) The increase in signal should be shut off as soon as the starvation condition is terminated by addition of the limiting nutrient

To determine if these criteria could be fulfilled, we started a fermentation with a low phosphate concentration and took out samples each hour for nine hours for different analyses:

1. 1) pstS and pstS-GFP mRNA levels determinations using Northern blot,
2. 2) off-line GFP concentration determinations,
3. 3) alkaline phosphatase activity determinations,
4. 4) FACS analysis,
5. 5) Inorganic phosphate concentration determinations.

The sampling was started four hours before we detected a signal of phosphate starvation. Fig. 1 shows how the spectra change during these nine hours. Fig. 2 show the data collected during these nine hours and the simultaneous increase in GFP signal (both on-line and off-line) and in alkaline phosphatase activity.

FACS analysis and microscopic examination of the samples showed induction of GFP production at the same time point, and very importantly, also showed that the whole population of cells reacted in the same manner (see fig. 3).

Most importantly, Northern blots showed that the pstS and the pstS-GFP are totally co-regulated, that we observe the GFP very shortly after we first detect the induction at the mRNA level, and finally, that addition of phosphate shuts off transcription of the promoter rapidly. Shutting down the promoter with phosphate also results in a stop in production of GFP about one hour after addition. This delay is probably an effect of a fairly stable pstS-GFP mRNA (a 5 to 10-fold reduction in pstS-GFP levels in 52 minutes after phosphate addition). Fig. 4. shows the on-line data on the change in GFP emission during 20 hours after sampling start. Here we see that the signal intensity stops to increase after about one hour after phosphate addition and that the intensity slowly drops. The added phosphate is probably consumed at about 42 h where the GFP signal again starts to increase.

To ensure that high biomass concentrations would not disturb the GFP signal, two more fermentations were run where one started with a low phosphate concentration (BPN102) and one with a high phosphate concentration (BPN101). The results are shown in fig. 6. No GFP induction occurs in BPN101, while a rapid GFP induction is seen in BPN102.

To test if we could induce a phosphate starvation in BPN101, about half the volume of the tank was exchanged with a medium that lacked phosphate at 47 hours into the fermentation. Shortly after, an increase in GFP signal was seen and 0.5 g phosphate was added. This stopped GFP production for 3 h and then, when the added phosphate was consumed, the GFP signal started to increase again.

Xylose utililization in B. subtilis requires the production of xylose isomerase (XylA) and xylulose kinase (XylB) and is regulated at the level of transcription by a xylose-responsive repressor protein encoded by xylR and by catabolite repression. Genes xylR and xylAB are divergently transcribed from a common intergenic region containing xyl operator sequences which are bound by xylR in the absence of an inducer. The xylose operon of B. subtilis is a well-characterized regulatory system with tight transcriptional regulation. Bhavsar et al (2001) developed a xylose-dependent system for expression of cloned genes from the amyE locus in B. subtilis. We have constructed a similar system for expression of cloned genes from the xyl locus in B. licheniformis Si3 strains.

The xylose locus was amplified from the chromosome of B. licheniformis Si3 and sequenced. Two regions were selected as targets for integration in the chromosome by double homologous recombination events. The upstream region (xyl-us) includes the 5'-end of the gene encoding the xylose repressor (xylR), intergenic xyl operator sequences, the xylA promoter, and the 5'-end of xylA encoding 21 aa followed by an artificial stop codon. The downstream region (xyl-ds) includes a xylB intragenic region.

The expression cassette contains four unique restriction sites but no Shine-Dalgarno sequence for translation of the cloned gene .

A gene selected for cloning and xylose-dependent expression therefore needs to bring its own Shine-Dalgarno sequence. This can easily be achieved by careful primer design and PCR amplification, the upstream primer should have an extra sequence with a recognition site for cloning, the SD-sequence, and the start codon for the gene to be expressed. The downstream primer should contain a stop codon but not a terminator sequence since this would prevent co-expression with the GFP-encoding BioST expression reporter-gene in the construct.

The resulting cloning expression vector was denoted pAN238 (Figure 7), cloning of an amplified "gene X" in pAN238 ensures its co-expression with BioST. Integration of the expression cassette into the chromosome of B. licheniformis by a double cross-over event will restore xylR but inactivate xylAB by serious truncation. The cloned gene will be expressed in the presence of xylose together with BioST. The full DNA sequence of pAN238 is provided in SEQ ID NO: 1.

In the first cloning strategy we inserted both nucB genes each into the pAN238 vector designed for integration into the xyl locus in B. licheniformis.

This integration allowed for induction of the nucB expression by adding xylose to the medium, since the nucB gene is under control of the xyl promoter. However, as a free plasmid in B. subtilis the xyl promoter will be constitutively active because the XylR repressor is out-titrated and it was expected that nucB would be fully expressed under these conditions. The two nucB genes were each amplified by PCR and cloned into the plasmid.

• Primer 480596 (SEQ ID NO: 2): TTTATTATCGATCAAGAGGAGGTTGTTTTTGTCATGATC
• Primer 480597 (SEQ ID NO: 3): TTTATTACGCGTATCCCCCACAACGATTTTCCTGTC

• Primer 480598 (SEQ ID NO: 4): TTATTTATCGATAAGGTATGGGGGGATGGGGATGAAAAAATGG
• Primer 480599 (SEQ ID NO: 5): TTATTTACGCGTCAGCTCGGCGAAGGATTGTAACAAC

These plasmids were each transformed into B. subtilis and plasmid preps were made. Restriction digests of the plasmids showed major break down of DNA which indicated that both the B. subtilis and B. licheniformis nucB genes were fully induced and the encoded nucleases could both be expressed into the medium. The two strains were kept as:

• MOL2676 (B. lich. nucB) pMOL2676
• MOL2677 (B. sub. nucB) pMOL2677

• MOL2680 (B. lich. nucB) pMOL2676
• MOL2681 (B. sub. nucB) pMOL2677

In a more controlled experiment, we inoculated the strains in TY, incubated at 37°C overnight, and mixed cell free 10 microliters of supernatant with marker DNA (1 Kb ladder). The samples were incubated at 37°C for different time intervals. There was major degradation of the marker DNA for the strain with the cloned nucB genes as compared to the control strains. The conclusion was that the nucB genes can both be expressed into functional nucleases in B. subtilis.

The second cloning strategy was to exploit the tightly controlled pstS promoter from B. licheniformis to express the nuclease under phosphate limited conditions, such as towards the end of a fermentation. Again, both of the nucB genes were amplified by PCR and cloned together with the pstS promoter into another plasmid pAN167, that was designed for integration into the pel locus in the B. subtilis chromosome. The DNA sequence of pAN167 is provided in SEQ ID NO: 6, and the restriction map is shown in figure 8.

• Primer Cat,aa49,forw (SEQ ID NO: 7): CCTTTATTAATGAATTTTCCTGCTG
• Primer GFP,aa17,rev (SEQ ID NO: 8): CAACAAGAATTGGGACAACTCCAGTG

• Primer 491264 (SEQ ID NO: 9): TTTATTACGCGTCAAGAGGAGGTTGTTTTTGTCATGATC
• Primer 492902 (SEQ ID NO: 10): TTTATTAAGCTTATCCCCCACAACGATTTTCCTGTC

• Primer 491266 (SEQ ID NO: 11): TTATTTACGCGTAAGGTATGGGGGGATGGGGATGAAAAAATGG
• Primer 492903 (SEQ ID NO: 12): TTATTTAAGCTTCAGCTCGGCGAAGGATTGTAACAAC

The ligations were transformed into B. subtilis and plasmid preps were made. Restriction digests showed the correct cloning had taken place. The nucB expression cassette with the pst promoter was integrated in the pel locus by double cross-over recombination and correct integration was verified by PCR. The following strains were preserved:

• MOL2684, MOL2685: integration of construct with nucB from B. licheniformis
• MOL2686, MOL2687: integration of construct with nucB from B. subtilis

In order to study if the pst promoter was able to activate the nucB gene at low phosphate concentration, a series of samples was set up. The two strains MOL2684 and MOL2686 were innoculated in TY medium with and without added phosphate. After an overnight growth at 37°C, the cells were pelleted and the supernatant was examined for nuclease activity by mixing it with marker DNA according to figure 9. 10 microliters of cellfree supernatant was applied with marker DNA (1 Kb ladder). The samples were incubated at 37°C for different time intervals.

As seen in fig. 9 there is major degradation of the marker DNA for the strain with the cloned B. licheniformis nucB gene as compared to the control strains, but only in fermentations without added phosphate. In fermentations with a surplus of phospate there is no trace of degradation.

The conclusion is that the nucB gene from B. licheniformis can be expressed from the Ppst promoter and is tightly controlled by the level of phophate in the medium.

We wanted to test the Ppst-nucB construct in a relevant amylase production strain used for expression of food enzymes, in commercially relevant fermentation conditions.

Chromosomal DNA from strain MOL2684 and MOL2685 was used to transform the production strain, selecting for chloramphenicol resistance. The presence of the nucB expression cassette was verified by PCR.

The resulting strains expressing nucB from the Ppst promoter integrated into the pel locus were preserved as: MOL2716, MOL2717, MOL2718 (integration of construct with nucB from B. licheniformis).

One of the resulting strains, MOL2717, was then fermented in 1 liter scale to investigate if the initiation of expression and activity of the NucB nuclease was sufficient to digest DNA. The fermentation was run as a phosphatase limited process through a four day fermentation and samples were taken each day. The samples were cleared for cells by centrifugation and mixed with marker DNA to examine the DNase activity. Results from this experiment are shown in figure 10. The lanes with samples from 1 litre scale fermentations show a slow degradation of DNA compared to earlier experiments, but after 240 min there is marked digestion of DNA resulting in diffuse bands. The controls show the expected activity.

• <110> Novozymes A/S
• <120> DNase Expression in Recombinant Host Cells
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